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线性分子式:
NH2(CH2)6NH2
化学文摘社编号:
分子量:
116.20
EC Number:
204-679-6
UNSPSC Code:
12352116
PubChem Substance ID:
Beilstein/REAXYS Number:
1098307
MDL number:
Assay:
≥98.0%
Grade:
SAJ first grade
InChI
1S/C6H16N2/c7-5-3-1-2-4-6-8/h1-8H2
InChI key
NAQMVNRVTILPCV-UHFFFAOYSA-N
SMILES string
NCCCCCCN
grade
SAJ first grade
vapor density
4 (vs air)
assay
≥98.0%
form
solid
expl. lim.
6.3 %
availability
available only in Japan
dilution
(for analytical testing)
refractive index
n20/D 1.439 (lit.)
pH
12.4 (25 °C, 100 g/L)
mp
42-45 °C (lit.)
density
0.89 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
176.0 °F - closed cup
flash_point_c
80 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
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Linda G T Gaines et al.
Journal of environmental monitoring : JEM, 13(1), 119-127 (2010-10-28)
Although urinary 1,6-hexamethylene diamine (HDA) is a useful biomarker of exposure to 1,6-hexamethylene diisocyanate (HDI), a large degree of unexplained intra- and inter-individual variability exists between estimated HDI exposure and urine HDA levels. We investigated the effect of individual and
Richard F G Fröhlich et al.
Carbohydrate research, 346(12), 1592-1598 (2011-06-08)
Two simple and reliably accessible intermediates, N-carboxypentyl- and N-aminohexyl-1-deoxy-D-galactonojirimycin were employed for the synthesis of a set of terminally N-dansyl substituted derivatives. Reaction of the terminal carboxylic acid of N-carboxypentyl-1-deoxy-D-galactonojirimycin with N-dansyl-1,6-diaminohexane provided the chain-extended fluorescent derivative. Employing bis(6-dansylaminohexyl)amine, the
Wei-Chiang Chen et al.
ACS applied materials & interfaces, 1(8), 1821-1826 (2010-04-02)
Solvent microenvironments are formed around individual single-walled carbon nanotubes (SWNTs) by mixing SWNT suspensions with water-immiscible organic solvents. These microenvironments are used to encapsulate the SWNTs with the monomer sebacoyl chloride. Hexamethylene diamine is then injected into the aqueous phase
Junseok Yeom et al.
Bioconjugate chemistry, 21(2), 240-247 (2010-01-19)
A novel, biocompatible, and nontoxic dermal filler using hyaluronic acid (HA) hydrogels was successfully developed for tissue augmentation applications. Instead of using highly reactive cross-linkers such as divinyl sulfone (DVS) for Hylaform, 1,4-butanediol diglycidyl ether (BDDE) for Restylane, and 1,2,7,8-diepoxyoctane
Linda G T Gaines et al.
The Annals of occupational hygiene, 54(6), 678-691 (2010-06-10)
Urinary 1,6-hexamethylene diamine (HDA) may serve as a biomarker for systemic exposure to 1,6-hexamethylene diisocyanate (HDI) in occupationally exposed populations. However, the quantitative relationships between dermal and inhalation exposure to HDI and urine HDA levels have not been established. We
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